Hemophagocytic Lymphohistiocytosis Secondary to Chronic Lymphocytic Leukemia Progression

Hemophagocytic lymphohistiocytosis (HLH) is an acute, rare systemic hyperinflammatory disorder caused by a dysregulated immune cell function and massive cytokine release, often leading to multiple organ involvement and failure. Fever, hepatosplenomegaly, cytopenia, elevated liver enzymes, hypertrigl...

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Detalles Bibliográficos
Autores principales: Jancar, Nina, Sousa Gonçalves, Filipa, Duro, José Fragoso, Aguiar, Patrício, Jacinto Correia, Catarina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Internal Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9949745/
https://www.ncbi.nlm.nih.gov/pubmed/36843678
http://dx.doi.org/10.7759/cureus.34128

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9949745/
https://www.ncbi.nlm.nih.gov/pubmed/36843678
http://dx.doi.org/10.7759/cureus.34128

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